Busse R, Fichtner H, Lückhoff A, Kohlhardt M
Department of Applied Physiology, University of Freiburg, Federal Republic of Germany.
Am J Physiol. 1988 Oct;255(4 Pt 2):H965-9. doi: 10.1152/ajpheart.1988.255.4.H965.
In freshly harvested aortic endothelial cells from rabbits, some cellular events associated with stimulation by acetylcholine (ACh) were analyzed. ACh (3 microM) induced a transient hyperpolarization of 8.3 +/- 2.5 mV, which peaked within 3-5 s and subsequently declined with a similar time course. Hyperpolarization was caused by a transient Ca2+-dependent outward current (IoACh), which was mainly carried by K+. ACh (3 and 10 microM) also evoked transient dose-dependent increases in the intracellular free Ca2+ concentration (Ca2+i). Pretreatment with atropine (1 and 3 microM) abolished both responses to ACh, the increase in Ca2+i as well as the transient outward current. It is concluded that IoACh and the rise in Ca2+i are two manifestations of muscarinic receptor stimulation. The rise in Ca2+i might be the primary event, leading to secondary membrane hyperpolarization.
对刚从兔体内获取的主动脉内皮细胞中一些与乙酰胆碱(ACh)刺激相关的细胞事件进行了分析。ACh(3微摩尔)诱导了8.3±2.5毫伏的瞬时超极化,在3 - 5秒内达到峰值,随后以类似的时间进程下降。超极化由瞬时钙依赖性外向电流(IoACh)引起,该电流主要由钾离子携带。ACh(3和10微摩尔)还引起细胞内游离钙浓度(Ca2+i)的瞬时剂量依赖性增加。用阿托品(1和3微摩尔)预处理可消除对ACh的两种反应,即Ca2+i的增加以及瞬时外向电流。得出的结论是,IoACh和Ca2+i的升高是毒蕈碱受体刺激的两种表现形式。Ca2+i的升高可能是主要事件,导致继发性膜超极化。